In vitro activity of ceftaroline against staphylococci from prosthetic joint infection

Kyung-Hwa Park1, Kerryl E Greenwood-Quaintance2, Robin Patel3

  • 1Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905; Department of Infectious Diseases, Chonnam National University Medical School, Gwangju, South Korea.

Insights

Ceftaroline effectively inhibited all staphylococci, including methicillin-resistant strains, in vitro. This suggests ceftaroline

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Prosthetic joint infections (PJIs) are often caused by Staphylococcus species.
  • Methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus epidermidis (MRSE) pose significant treatment challenges.
  • Novel antimicrobial agents are needed for effective PJI management.

Purpose of the Study:

  • To evaluate the in vitro activity of ceftaroline against staphylococci isolated from patients with PJIs.
  • To determine the susceptibility of both methicillin-susceptible and methicillin-resistant staphylococcal strains to ceftaroline.

Main Methods:

  • Etest method was employed to determine the minimum inhibitory concentrations (MICs) of ceftaroline.
  • Staphylococcal isolates were recovered from patients diagnosed with prosthetic joint infections.
  • Isolates included Staphylococcus aureus and Staphylococcus epidermidis, with varying oxacillin resistance profiles.

Main Results:

  • Ceftaroline demonstrated potent in vitro activity against all tested staphylococcal isolates, inhibiting growth at concentrations ≤0.5 μg/mL.
  • MIC(90/50) values for ceftaroline ranged from 0.094/0.047 μg/mL (methicillin-susceptible S. epidermidis) to 0.5/0.38 μg/mL (methicillin-resistant S. aureus).
  • All isolates, including MRSA and MRSE, were susceptible to ceftaroline at clinically relevant concentrations.

Conclusions:

  • Ceftaroline exhibits significant in vitro efficacy against a broad spectrum of staphylococci implicated in PJIs.
  • These findings support the further investigation of ceftaroline as a therapeutic agent for staphylococcal PJIs.
  • Ceftaroline represents a promising option for treating infections caused by both methicillin-susceptible and methicillin-resistant staphylococci.

Related Concept Videos

Staphylococcal Skin Infections01:29

Staphylococcal Skin Infections

Staphylococcus aureus is a Gram-positive coccus that resides harmlessly on the skin and mucous membranes of healthy individuals. When the skin barrier is breached, it can shift from a commensal to an opportunistic pathogen. This transition is facilitated by surface adhesins, such as clumping factor B and S. aureus surface protein G (SasG), which bind to structural proteins, including loricrin and cytokeratin, in the damaged epidermis. Protein A, another key factor, binds the Fc region of...
62
Clinical Significance of Antibiotic Resistance01:25

Clinical Significance of Antibiotic Resistance

Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within...
32
Antimicrobial Effectiveness01:28

Antimicrobial Effectiveness

The effectiveness of antimicrobial agents depends on various factors influencing their ability to eliminate microbial populations. Larger microbial populations require more time for complete eradication, emphasizing the importance of population size analysis when evaluating antimicrobial efficacy.Microbial resistance to antimicrobial agents varies significantly. Highly resilient microorganisms include endospores, gram-negative bacteria, and non-enveloped viruses, while prions are exceptionally...
2.0K
Mechanism of Antibiotic Resistance in MRSA01:25

Mechanism of Antibiotic Resistance in MRSA

Antibiotic resistance in bacteria arises when microorganisms evolve the ability to withstand drugs designed to kill them or inhibit their growth, rendering once-effective treatments useless. This phenomenon, driven by genetic change and selection under antibiotic exposure, poses a profound threat to modern medicine. Mechanisms include drug-inactivating enzymes (e.g., β-lactamases), efflux pumps that eject antibiotics, mutations altering antibiotic targets, decreased drug uptake, and...
99